Search Results (3,439)

The objective of this study was to assess the content of selected elements—fluorine, calcium and inorganic phosphorus—in infusions prepared from selected commercial leaf teas available on the Polish market. A comprehensive analysis was conducted based on tea type and geographical origin. In addition, the Target Hazard Quotient (THQ) was calculated to estimate the non-carcinogenic health risk associated with fluoride intake from tea consumption. Methods: A total of 98 leaf tea samples were analyzed, including 55 black, 27 green, 9 oolong, and 7 white teas. Standardized brewing protocols were applied. Measured parameters included pH, calcium and inorganic phosphorus content, buffer capacity, and titratable acidity. Fluoride concentrations were determined using an ion-selective electrode. Statistical analysis was performed using non-parametric methods (Kruskal–Wallis ANOVA with DSCF post hoc test), and heatmaps were generated to illustrate the distribution of THQ across different models. Results: Black teas exhibited significantly lower pH values and higher titratable acidity, buffer capacity, and inorganic phosphorus levels compared to other tea types, indicating distinct physicochemical properties. Although all THQ values for fluoride remained well below the safety threshold (THQ < 1), the highest values were observed in elderly individuals with low body weight, particularly women consuming green tea, suggesting increased vulnerability in this subgroup. Conclusions: Among the analyzed samples, black teas demonstrated the most distinct chemical profile, characterized by the lowest pH and the highest acidity, buffer capacity, and fluoride and phosphorus content—especially in teas originating from Africa and Central Asia. While fluoride exposure from leaf tea infusions does not appear to pose a direct health risk, older adults, particularly low-weight women, may be more susceptible to potential non-carcinogenic effects and should moderate their intake of high-fluoride teas. Full article

Despite notable advancements in lithium-ion battery (LIB) technology, growing industrialization, rising energy demands, and evolving consumer electronics continue to raise performance requirements. As the primary determinant of battery performance, cathode materials have become a central research focus. Among emerging candidates, iron-based fluorides show great promise due to their high theoretical specific capacities, elevated operating voltages, low cost (owing to abundant iron and fluorine), and structurally diverse crystalline forms such as pyrochlore and tungsten bronze types. These features make them strong contenders for next-generation high-energy, low-cost LIBs. This review highlights recent progress in iron-based fluoride cathode materials, with an emphasis on structural regulation and performance enhancement strategies. Using pyrochlore-type hydrated iron trifluoride (Fe₂F₅·H₂O), synthesized via ionic liquids like BmimBF₄, as a representative example, we discuss key methods for tuning physicochemical properties—such as electronic conductivity, ion diffusion, and structural stability—via doping, compositing, nanostructuring, and surface engineering. Advanced characterization tools (XRD, SEM/TEM, XPS, Raman, synchrotron radiation) and electrochemical analyses are used to reveal structure–property–performance relationships. Finally, we explore current challenges and future directions to guide the practical deployment of iron-based fluorides in LIBs. This review provides theoretical insights for designing high-performance, cost-effective cathode materials. Full article

Hydrogen-induced steel embrittlement imposes a technical difficulty in facilitating effective and safe hydrogen transportation via pipelines. This investigative study assesses the potency of polyvinylidene fluoride (PVDF)–graphene-based composite coatings in the inhibition of hydrogen permeation. Spin coating was the method selected for this study, and varying graphene concentrations ranging from 0.1 to 1wt% were selected and applied to 306 stainless steel substrates. A membrane permeation cell was used in the evaluation of hydrogen permeability, while the impact of graphene loading on coating performance was analyzed using the response surface methodology (RSM). The outcomes showed an inversely proportional relationship between the graphene concentration and hydrogen ingress. The permeation coefficient for pure PVDF was recorded as 16.74, which decreased to 14.23, 12.10, and 11.46 for 0.3, 0.5, and 1.0 wt% PVDF-G, respectively, with the maximum reduction of 31.6% observed at 1.0 wt%. ANOVA established statistical significance, along with indications of strong projection dependability. However, the inhibition reduction stabilized with increasing graphene concentrations, likely caused by nanoparticle agglomeration. The results support the notion of PVDF–graphene’s potential as a suitable coating for the transformation of pipelines for hydrogen transport infrastructure. This research will aid in the establishment of suitable contemporary barrier coating materials, which will enable the safe utilization of hydrogen energy in the current energy transportation grid. Full article

Background: Dental caries is a prevalent dental problem affecting primary and permanent teeth. Early demineralization of enamel lesions can be reversed through remineralization. Many studies have focused on caries prevention and disease progression arrest using silver diamine fluoride (SDF). No in vitro studies have compared the remineralization effects of different 38% SDF solutions on artificially demineralized enamel lesions. This study aimed to compare the remineralization potential of three commercial 38% silver diamine fluoride formulations on artificial enamel lesions in primary teeth using a pH cycling model. The hypothesis was as follows: different commercial SDF formulations would exhibit varying remineralization effects, as measured by surface microhardness, due to potential differences in their compositions. Materials and Methods: In this study, 75 primary molars were randomized into five groups (N = 15): I: baseline, II: SDF Riva Star Aqua^® 38%, III: Riva Star^® 38%, IV: SDF Advantage Arrest^® 38%, and V: control. Artificial caries were created by submerging teeth in 10 mL of demineralization solution (pH 4.5) for three days in a light-resistant container, ensuring distinct visual changes in the enamel as per the International Caries Detection and Assessment System (ICDAS level 2). After pH cycling, all samples underwent a standardized Vickers microhardness test (VMHT) with a 50 g load for 15 s. Data were analyzed using one-way ANOVA and Tukey’s post hoc test, with a significance level set at p ≤ 0.05. Results: The one-way ANOVA test indicated a significant difference in microhardness among the groups (SDF Riva Star Aqua, SDF Riva Star, and SDF Advantage Arrest), with an F-value of 167.73 and p < 0.001. The post hoc Scheffé test showed that SDF Riva Star Aqua and SDF Riva Star were not significantly different (p = 0.388). However, SDF Advantage Arrest had a significantly higher mean microhardness compared to both groups (p < 0.001). Overall, these results show that SDF Advantage Arrest leads to greater microhardness than SDF Riva Star Aqua or SDF Riva Star. Conclusions: SDF Advantage Arrest showed superior performance among the SDF-treated groups, significantly increasing microhardness compared to SDF Riva Star Aqua and SDF Riva Star. This suggests that SDF Advantage Arrest offers enhanced remineralization and structural strengthening, making it the most effective option for managing demineralized primary teeth. Future research should investigate the long-term performance and mechanisms of these treatments to optimize clinical protocols for preserving primary tooth integrity. Full article

Polymer inclusion membranes (PIMs) have undergone substantial advancements in their selectivity and efficiency, driven by their increasing deployment in separation processes, environmental remediation, and sensing applications. This review presents recent progress in the development of PIMs, focusing on strategies to enhance ion and molecule selectivity through the incorporation of novel carriers, including ionic liquids and task-specific extractants, as well as through polymer functionalization techniques. Improvements in mechanical and chemical stability, achieved via the utilization of high-performance polymers such as polyvinylidene fluoride (PVDF) and polyether ether ketone (PEEK), as well as cross-linking approaches, are critically analyzed. The expanded application of PIMs in the removal of heavy metals, organic micropollutants, and gas separation, particularly for carbon dioxide capture, is discussed with an emphasis on efficiency and operational robustness. The integration of PIMs with electrochemical and optical transduction platforms for sensor development is also reviewed, highlighting enhancements in sensitivity, selectivity, and response time. Furthermore, emerging trends towards the fabrication of sustainable PIMs using biodegradable polymers and green solvents are evaluated. Advances in scalable manufacturing techniques, including phase inversion and electrospinning, are addressed, outlining pathways for the industrial translation of PIM technologies. The review concludes by identifying current limitations and proposing future research directions necessary to fully exploit the potential of PIMs in industrial and environmental sectors. Full article

Commercial hydrophobic membranes encounter severe problems such as membrane wetting and membrane fouling under extreme conditions, which affect membrane separation performance. To enhance the anti-fouling abilities of hydrophobic membranes, a composite membrane with omniphobic characteristics was fabricated successfully in this paper. Titanium dioxide (TiO₂) nanoparticles were in-situ grown via the hydrothermal synthesis method, and then fluorosilane with low surface energy was grafted on polyvinylidene fluoride (PVDF) membranes. Subsequently, the morphologies, chemical compositions, wetting properties and structural parameters of composite membranes were characterized systematically. Various contaminants were added to the feed to investigate the anti-fouling and anti-wetting performances of the composite membrane in membrane distillation tests. The results showed that butyl titanate was first hydrolyzed to form titanium hydroxide (Ti(OH)₄) and then it was dehydrated to form TiO₂ in the hydrothermal environment. TiO₂ crystals continued to grow and formed rough morphology with micro-nano synergistic distribution, which is similar to a “sunflower” disk composed of cubic clusters and nanopillars. Meanwhile, fluorosilane successfully was grafted onto TiO₂. The contact angles of deionized water, 0.4 mM sodium dodecyl sulfate (SDS) solution and 0.2% v/v mineral oil emulsion on the composite membrane surface were 167.3°, 162.0° and 158.5°, respectively, endowing the composite membrane with excellent omniphobic features. In direct contact membrane distillation (DCMD) tests, the composite membrane exhibited a relatively stable membrane permeate flux, and the salt rejection rate almost reached 100%. The mixture, consisting of inorganic salts, organic substances, surfactants and oil emulsions, was used as feed. In contrast, the commercial PVDF membrane flux decreased drastically and even dropped to 0 due to the membrane fouling and wetting. As for the pristine PVDF membrane, the membrane surface was covered with pollutants and membrane pores were blocked. Therefore, it was proved that the omniphobic composite membrane possesses outstanding anti-fouling and anti-wetting performance. Full article

This paper discusses the potential of adding a self-made super-early-strength agent to produce quick-setting, quick-hardening, and high-strength concrete. A super-early-strength agent is prepared by mixing triethanolamine (TEA), aluminum sulfate (Al₂(SO₄)₃·18H₂O), formic acid (HCOOH), and sodium fluoride (NaF) with a water-reducing agent in different proportions. In this paper, the effects of super-early-strength agent ratio and dosage, water–binder ratio, silica fume content, and cementitious material content on the setting time and compressive strength of high-strength concrete were studied. The hydration characteristics were evaluated by X-ray diffraction (XRD) and TG-DSC thermal analysis. The results show that the high-strength concrete prepared by 42.5R ordinary Portland cement mixed with appropriate amount of silica fume and self-made super-early-strength agent has a compressive strength of 10 MPa in 6 h, a compressive strength of 40 MPa in 1 day, a compressive strength of not less than 80 MPa in 28 days, and a compressive strength of not shrinking in 180 days. Using conventional raw materials and general process methods, the concrete prepared according to the preparation method of this experiment can significantly shorten the setting time and improve the compressive strength. However, it is difficult to form concrete when the amount of super-early-strength agent is too large. Nevertheless, this study provides a theoretical basis for large-scale and high-value utilization of the potential of super-early-strength agents and development to improve efficiency. At the same time, it provides a reference for the application of coating technology in rapid repair engineering. Full article

Crystal twinning, a common growth phenomenon, can substantially affect material performance in fields such as semiconductors, nonlinear optics, and drug development, yet its elimination during crystallization is challenging. This study presents a method for the controlled synthesis of ZSM-5 zeolite as either single crystals or twinned crystals using kaolin as the primary raw material. The method leverages the etching effect of ammonium fluoride (NH${⁠}_4$F) on the aluminosilicate structure derived from pre-treated kaolin. By adjusting the concentrations of NH${⁠}_4$F and the structure-directing agent tetrapropylammonium bromide (TPABr), pure ZSM-5 single crystals and twinned crystals were selectively synthesized. Conventionally, NH${⁠}_4$F is employed to introduce defects into zeolite structures. In contrast, this work demonstrates its utility in controlling crystal habit. The synthesis utilizes kaolin, an abundant and low-cost aluminosilicate mineral, to provide the entire aluminum source and a portion of the silicon source, offering an economical alternative to expensive precursors like aluminum isopropoxide. The resulting single and twinned crystals exhibited high crystallinity, demonstrating the viability of using natural minerals to produce high-quality zeolites. The physical and chemical properties of the kaolin-derived ZSM-5 were characterized and compared to those of ZSM-5 synthesized from conventional chemical reagents. A growth mechanism for the formation of single and twinned crystals is also proposed. Full article

Wastewater treatment plants generally lack a specialized design for the efficient removal of sulfamethoxazole (SMX), a toxic and bio-resistant compound. In this study, secondary effluent from a Beijing wastewater reclamation treatment plant was spiked with SMX and used to investigate the filtration performance and fouling mechanisms of thermo-responsive membranes. Thermo-responsive materials were prepared using polyvinylidene fluoride, N-isopropylacrylamide (NIPAM), and graphene oxide through Ce (IV)-induced redox radical polymerization. The results showed that the removal of SMX and COD reached 42% and 92%, respectively, with a NIPAM dosage of 1 g, and the removal of UV₂₅₄ reached its highest value at 57.9%. Additionally, the filtration flux was higher at a temperature of 35 °C with a NIPAM dosage of 1 g. The fluorescence intensity of the organic matter from the secondary effluent spiked with SMX and decreased after the thermo-responsive membranes were implemented, and filtration with the membrane containing 1 g of NIPAM achieved a lower intensity at a value of 3074.6, according to the analysis of three-dimensional fluorescence excitation–emission spectroscopy. According to the extended Derjaguin–Laudau–Verwey–Overbeek theory analysis, the interfacial free energies of the thermo-responsive membrane with a 1 g dose of NIPAM were higher than the others during filtration. Full article

The selectivity of the colorimetric method for Co(II) determination using the nitroso-R-salt (NRS) in samples with complex matrices has been improved. Interferences caused by Cu(II), Fe(II), Fe(III), Mn(II), Al(III) and Ni(II) ions, which were present in the bioleach ate of lithium-ion batteries, have been solved through the sequential addition of masking agents: acetate, fluoride, ethylenediaminetetraacetic acid (EDTA), and strong acids (H₂SO₄). The absorbance of the NRS-Co(II) complex was typically measured at 525 nm, but it was also studied at 550 nm due to minimal interferences observed at 550 nm. The sequence of the masking agent’s addition showed a significant influence on the interference effect. The optimal sequence was sample, acetate–acetic acid buffer solution with dissolved fluoride, NRS, EDTA and H₂SO₄. The proposed method demonstrated robust performance at 550 nm, with a relative standard deviation (RSD) around 2%, and good accuracy (RV% around 100%). The limit of detection (LoD) was 0.1 mg L⁻¹ and the limit of quantification (LoQ) was 0.3 mg L⁻¹. The linear range extended up to 15 mg L⁻¹ (R² = 0.998). Real samples analyzed using the optimized method showed no significant differences when compared to results from atomic absorption spectroscopy, confirming its reliability. Full article

In this study, a selection of active materials were coated onto commercially available intermediate modulus carbon fibers to form and analyze the performance of novel composite cathodes for structural power composites. Various slurries containing polyvinylidene fluoride (PVDF), active material powders, 1-methyl-2-pyrrolidone (NMP) and carbon black (CB) were used to coat carbon fiber tows by immersion. Four active materials—lithium cobalt oxide (LCO), lithium iron phosphate (LFP), lithium nickel manganese cobalt oxide (NMC), and lithium nickel cobalt aluminum oxide (NCA)—were individually tested to assess their electrochemical reversibility. The cells were prepared with a polymer separator and liquid electrolytes and assembled in 2025-coin cells. Electrochemical analysis of the cathode materials showed that at C/5 and room temperature the measured capacities ranged from 39.8 Ah kg⁻¹ to 64.7 Ah kg⁻¹ for the LFP and NCA active materials, respectively. The full cells exhibited capacities of 18.1, 23.5, 27.2, and 28.2 Ah kg⁻¹ after 55 cycles for LFP, LCO, NCA, and NMC811, respectively. Finally, visual and elemental analysis were performed via scanning electron microscope (SEM) and energy-dispersive x-ray (EDX) confirming desirable surface coverage and successful transfer of the active materials onto the carbon fiber tows. Full article

This study explores the enhancement of fluoride adsorption using biochar derived from the brown macroalga Sargassum polycystum, which was treated with iron oxide (Fe₃O₄). The macroalgal biomass underwent pyrolysis at 400 °C, followed by Fe₃O₄ impregnation, to improve surface functionality and create active sites for fluoride ion binding. Various factors affecting fluoride removal were systematically examined. A maximum fluoride removal effectiveness of 90.2% was attained under ideal circumstances (pH 2, 60 mg adsorbent dose, 30 mg/L fluoride concentration, and 150 min contact duration). Adsorption isotherm analysis showed that the Langmuir model provided a better fit (R² = 0.998) than the Freundlich model (R² = 0.941), with a maximum adsorption capacity (qₘ) of 3.41 mg/g, indicating monolayer adsorption on a homogeneous surface. Kinetic modeling revealed that the pseudo-second-order model best described the adsorption process (R² = 0.9943), suggesting chemisorption as the dominant mechanism, while the intraparticle diffusion model also showed a good fit (R² = 0.9524), implying its role in the rate-limiting step. Surface complexation, facilitated by the enhanced surface area and porosity of the iron-modified biochar, was identified as the primary mechanism of fluoride ion interaction. This study highlights the potential of Fe₃O₄-modified macroalgal biochar as an effective and sustainable solution for fluoride remediation in contaminated water sources. Full article

Hydrothermal scheelite from three Romanian occurrences was analyzed in order to ascertain its structural, physical, vibrational, paragenetic, and crystal-chemical peculiarities as an important tool for characterizing the metallogenetic behavior and facilitating the ore-processing. All three occurrences, i.e., Ciclova and Oravița in Banat and Băița Bihor in the Bihor Mountains, are related to skarn deposits developed at the contact of Upper Cretaceous granodioritic bodies with Mesozoic calcareous deposits. Typical crystals show {001}, {111}, and {101} forms and are up to 15 mm across. The structure was successfully refined as tetragonal, space group I4₁/a, with R₁ = 0.0165 (Ciclova), 0.0204 (Oravița), and 0.0237 (Băița Bihor), respectively. The cell parameters refined for the same samples are a = 5.2459(10) Å and c = 11.3777(5) Å at Ciclova, a = 5.2380(2) Å and c = 11.3679(8) Å at Oravița, and a = 5.2409(2) Å and c = 11.3705(6) Å at Băița Bihor. The multiplicity of bands in both infrared absorption and Raman spectra is consistent with the S₄ punctual symmetry of the tungstate anion, agreeing with the structural data. In all cases, the analyzed scheelite is close to the CaWO₄ end-member. Cathodoluminescence peculiarities at the level of single crystals suggest that they crystallized in a slightly oxidizing to reducing environment from late hydrothermal solutions. Textural and paragenetic peculiarities suggest that scheelite from the three occurrences crystallized from epithermal, low-temperature, fluoride- and boron-bearing aqueous solutions. Full article

Dental caries is now recognised as a multifactorial disease shaped by complex interactions among genetic, epigenetic, microbiological, environmental, and social factors. This narrative review synthesises recent findings on the influence of genetic and epigenetic factors on caries susceptibility, exploring implications for personalised prevention strategies, including novel vaccine approaches. Numerous gene polymorphisms in pathways related to enamel formation, saliva composition, immune response, and taste perception have been linked to increased caries risk, with some effects modulated by sex and tooth-specific factors. Early-life environmental exposures (diet, tobacco, and antibiotic use) have been demonstrated to further alter risk through epigenetic modifications such as DNA methylation, microRNA regulation, and histone changes. The recognition of this landscape of inherited and acquired vulnerabilities has given rise to interest in innovative preventive measures. In particular, anti-caries vaccines targeting Streptococcus mutans are being developed using protein subunits, DNA constructs, and even plant-based antigen production. Notwithstanding the challenges that still need to be overcome—chiefly the achievement of robust mucosal immunity, the assurance of safety, and the enhancement of production—these vaccines are proving to be a promising addition to traditional oral hygiene and fluoride measures. The integration of genetic and epigenetic insights with immunological advances has the potential to facilitate the development of more effective, personalised interventions to prevent dental caries. Full article